Peter Bowers

post-doc

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Roessler E, Pei W, Ouspenskaia MV, et al. (2009) Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly. Molecular Genetics and Metabolism. 98: 225-34
Roessler E, Ouspenskaia MV, Karkera JD, et al. (2008) Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly. American Journal of Human Genetics. 83: 18-29
Grossman HA, Goon B, Bowers P, et al. (2003) Once-weekly epoetin alfa dosing is as effective as three times-weekly dosing in increasing hemoglobin levels and is associated with improved quality of life in anemic HIV-infected patients. Journal of Acquired Immune Deficiency Syndromes (1999). 34: 368-78
Bamford RN, Roessler E, Burdine RD, et al. (2000) Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects. Nature Genetics. 26: 365-9